CCZ1 antibody (Cy7)

Catalog No. ABIN1421198

The Rabbit Polyclonal anti-CCZ1 antibody is suitable to detect CCZ1 in samples from Human, Mouse and Rat. It has been validated for WB and IF (p).

Quick Overview for CCZ1 antibody (Cy7) (ABIN1421198)

Target: CCZ1 (CCZ1 Vacuolar Protein Trafficking and Biogenesis Associated Homolog (S. Cerevisiae) (CCZ1))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CCZ1 antibody is conjugated to Cy7

Application: Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Product Details anti-CCZ1 Antibody (Cy7)

Cross-Reactivity: Human, Mouse, Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human CCZ1

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Expiry Date: 12 months

Target Details for CCZ1

Target: CCZ1 (CCZ1 Vacuolar Protein Trafficking and Biogenesis Associated Homolog (S. Cerevisiae) (CCZ1))

Alternative Name: CCZ1

Background:

Synonyms: C7orf28A, CCZ1 vacuolar protein trafficking and biogenesis associated homolog S. cerevisiae, CCZ1A, CGI-43, H_DJ1163J12.2, Vacuolar fusion protein CCZ1 homolog, CCZ1_HUMAN.

Background: Chromosome 7 is about 158 milllion bases long, encodes over 1000 genes and makes up about 5 % of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf28 gene product has been provisionally designated C7orf28 pending further characterization.